Genopathy
Gene-Disorder Association · Article
Gene
TAPBPL
TAP Binding Protein Like
Disorder
Congenital Myasthenic Syndrome
First reported 1951
Key publication · disorder Congenital myasthenia gravis.Archives of disease in childhood · 1951
Association Review

In brief

The association between TAPBPL (TAP Binding Protein Like) and Congenital Myasthenic Syndrome is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 1
Symptoms 71
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
TAPBPL

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Congenital Myasthenic Syndrome

The disorder

10 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

68 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

1 clinical variant

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Provenance

References & sources

6 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access